Thesis (Ph. D.)--University of Texas at Austin, 2003. / Vita. Includes bibliographical references. Available also from UMI Company.

Thesis--Ph. D., University of Hong Kong. / Mimeographed.

Thesis--Ph. D., University of Hong Kong. / Typewritten.

Thesis (M.Sc.)--Memorial University of Newfoundland, 2002. / Includes bibliographical references.

published_or_final_version / Medicine / Doctoral / Doctor of Philosophy

Not available / text

A large-scale pilot plant (0.43 m ID) was extensively modified and converted into an absorber/stripper system to demonstrate CO₂ capture technology using aqueous piperazine promoted potassium carbonate for coalfired power plants. Four pilot plant campaigns were completed. Three campaigns were conducted using 5 m K⁺/2.5 m PZ and 6.4 m K⁺/1.6 m PZ. Flexipac 1Y and Flexipac AQ Style 20 structured packing were used in the absorber. The stripper was tested with 14 sieve trays, IMTP #40 random packing, and Flexipac AQ Style 20 packing. Monoethanolamine (7 m) was tested in the third campaign to establish a base case. An approximate rate analysis showed that 5 m K⁺/2.5 m PZ is two times faster than 7 m MEA and three times faster than 6.4 m K⁺/1.6 m PZ. The location of the temperature bulge moves from the top of the column to bottom as the liquid to gas flow rate ratio is increased. Foaming occurred in the absorber in the first two campaigns and occurred in the stripper in the fourth campaign. Data from the pilot plant was used to develop a K⁺/PZ absorber model in Aspen Plus® RateSep[trademark]. The Hilliard (2005) Aspen Plus® VLE model and the kinetics developed by Cullinane (2005) were incorporated in the model. Data-Fit was simultaneously used to reconcile pilot plant data and perform a regression of the interfacial area and heat loss parameters for the RateSep[trademark] absorber model. The lean loading for the pilot plant data was shifted down by 10% to account for a discrepancy with the Cullinane vapor-liquid equilibrium data. The Data-Fit results showed that the average interfacial area for Flexipac 1Y was 80% of the value measure by the air-water column. The average interfacial area for Flexipac AQ Style 20 for 5 m K⁺/2.5 m PZ was 56% of the air-water measurement. The CO₂ heat of absorption may not have been adequately predicted by the RateSep[trademark] absorber model because the regressed values of heat loss were consistent with forced convection.

No description available.

Diversity in the expression of ion channel proteins among neurons allows a wide range of excitability, growth and functional regulation. Ether-a-go-go (EAG), a member of the voltage-gated K+ channels, was characterized by spontaneous firing in nerve terminals and enhanced neurotransmitter release. In situ whole-cell patch-clamp recordings performed from the somata of Drosophila larval thoracic aCC motoneurons revealed spontaneous spike-like events in eag mutants. Spontaneous events were absent in wild type motoneurons. Spikes evoked by somatic current injection in to the cell body were not altered and comparable to wild type. Spontaneous spike-like events could be due to increased synaptic drive or altered intrinsic excitability of the motoneuron. Reduction of EAG function with selective expression of eag double stranded RNAi transgene in motoneurons only did not cause spontaneous spike-like events or alter evoked firing. This suggests increased synaptic drive contributes to spontaneous events.Both transient and sustained voltage-activated K+ currents, each with Ca++-sensitive (IA(Ca) and IK(Ca)) and Ca++ -insensitive components (IA and IK), were isolated in thoracic aCC motoneurons. In wild type motoneurons, IA was larger than IA(Ca). Conversely, IK(Ca) was larger than IK. Both eag mutants and eag RNAi expression resulted in a decrease in IA , IK and a slow sustained K+ current. Further, EAG and Shal demonstrate a potential functional interaction and contribute to IA. The voltage sensitivity for inactivation was reduced in Shal only and EAG-Shal double knock down compared to controls and EAG only knock down. In addition, a Ca++ sensitive EAG dependent K+ current was blocked by cAMP. Thus, both voltage-dependent and modulatory functions of EAG influence excitability in motoneurons.Firing properties and K+ currents distinguish aCC motoneurons in thoracic segments, T1 and T3. T3aCC had a shorter delay to spike, higher input resistance and were more easily recruited than T1aCC. T1aCC had a larger IA than T3aCC, but comparable IA(Ca). IK(Ca) was larger in T3aCC compared to T1aCC. These differences reflect cell-specific ion channel distribution that could contribute to patterned segmental motor output.

The processing of sensory signals is an important, yet complex task in which a system must extract behaviorally relevant stimulus patterns from a vast array of sensory cues. When a neuron within a major sensory area is presented with a stimulus, one of the important characteristics used to distinguish between types of input is frequency. Often sensory neurons are tuned to narrow stimulus frequency ranges and are thus charged with the processing of subtypes of sensory signals. The weakly electric fish Apteronotus lepthorhynchus senses it's environment through modulations of a self-generated electric field. Two main types of sensory signals can be distinguished based on their frequency patterns. Prey stimuli cause low frequency perturbations of the electric field, while communication signals often result in high frequency signals. Pyramidal neurons in the electrosensory lateral line lobe (ELL) encode the low frequency signals with bursts, while the high frequency signals are relayed with single spikes. This thesis describes how a pyramidal neuron's response patterns can be tuned to specific frequencies by the expression of distinct classes of potassium channels. / I have cloned 3 small conductance (SK) calcium activated potassium channels from cDNA libraries created from the brain of Apteronotus. I have subsequently localized the AptSK channels throughout the brain using both in situ hybridization (AptSK1, 2 & 3) and immunohistochemical (AptSK1 & 2) techniques. The 3 channels showed distinct expression patterns, with the AptSK1 & 2 channels showing a partially overlapping expression pattern, while AptSK3 appears to be expressed in unique areas of the brain. In the ELL AptSK1 & 2 show a partially overlapping expression pattern, appearing in similar pyramidal neurons. However, their distribution within individual cell is unique, with AptSK1 showing a dendritic localization, while AptSK2 is primarily somatic. We have demonstrated that the unique expression pattern of the somatic AptSK2 channel in the ELL coincides with the functional SK currents evaluated through in vitro electrophysiology. Further we have shown that neurons that encode low frequencies do not possess functional SK channels. It thus appears that the presence of the AptSK2 channel subtype can predispose a neuron to respond to specific types of sensory signals. / In an attempt to evaluate if second messengers could modify the AptSK control of frequency tuning I investigated the consequences of muscarinic acetylcholine receptor (mAChR) activation on a pyramidal neurons response patterns. While it had been shown in vivo that mAChR activation increased a pyramidal neuron's response to low frequencies, I have found that this was not due to a decrease in AptSK current, but rather appears to be the result of a down-regulation of an A-type potassium channel. / Taken together the studies that comprise this thesis show how the selective expression of a single potassium channel subtype can control a sensory neurons response to specific environmental cues. The secondary modulation of the A-type current highlights the potential for a second messenger to control a neuron's sensory response through the down-regulation of constitutively expressed potassium current.